| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| P A Crossey, E R Maher, M H Jones, F M Richards, F Latif, M E Phipps, M Lush, K Foster, K Tory, J S Gree. Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus. Human molecular genetics. vol 2. issue 3. 1993-06-29. PMID:8499917. |
genetic linkage between von hippel-lindau disease and three microsatellite polymorphisms refines the localisation of the vhl locus. |
1993-06-29 |
2023-08-12 |
Not clear |
| J R Ortaldo, G M Glenn, H A Young, J L Fre. Natural killer (NK) cell lytic dysfunction and putative NK cell receptor expression abnormality in members of a family with chromosome 3p-linked von Hippel-Lindau disease. Journal of the National Cancer Institute. vol 84. issue 24. 1993-01-11. PMID:1460671. |
individuals susceptible to or clinically manifesting von hippel-lindau disease (vhl) have a genetic defect telomeric to this region on chromosome 3. |
1993-01-11 |
2023-08-11 |
human |
| G Kovacs, A Emanuel, H P Neumann, H F Kun. Cytogenetics of renal cell carcinomas associated with von Hippel-Lindau disease. Genes, chromosomes & cancer. vol 3. issue 4. 1992-01-06. PMID:1958591. |
to establish the chromosome pattern, we have analyzed short-term cultures of 24 renal cell carcinomas (rcc) from four patients with von hippel-lindau disease (vhl). |
1992-01-06 |
2023-08-11 |
Not clear |
| G M Glenn, L N Daniel, P Choyke, W M Linehan, E Oldfield, M B Gorin, S Hosoe, F Latif, G Weiss, M Walthe. Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus. Human genetics. vol 87. issue 2. 1991-08-13. PMID:2066108. |
as part of an attempt to locate the von hippel-lindau locus (vhl) on chromosome 3, we evaluated 41 families with von hippel-lindau disease from the united states and canada. |
1991-08-13 |
2023-08-11 |
Not clear |
| C H Mart. von Hippel-Lindau disease: a genetic condition predisposing tumor formation. Oncology nursing forum. vol 18. issue 3. 1991-07-26. PMID:2057398. |
von hippel-lindau disease (vhl) is a rare, autosomal, dominantly transmitted disease that genetically predisposes affected people to tumor development. |
1991-07-26 |
2023-08-11 |
Not clear |
| B R Seizinge. Toward the isolation of the primary genetic defect in von Hippel-Lindau disease. Annals of the New York Academy of Sciences. vol 615. 1991-07-02. PMID:2039154. |
von hippel-lindau disease (vhl) is a devastating hereditary tumor syndrome associated with various forms of cancer in multiple organ systems, including endothelial-derived tumors in the central nervous system, pheochromocytomas, and, a particularly frequent cause of death in vhl, renal cell carcinomas. |
1991-07-02 |
2023-08-11 |
Not clear |
| D L Miller, P L Choyke, M M Walther, J L Doppman, P J Kragel, G H Weiss, W M Lineha. von Hippel-Lindau disease: inadequacy of angiography for identification of renal cancers. Radiology. vol 179. issue 3. 1991-06-13. PMID:2028001. |
selective renal angiograms were retrospectively evaluated for the identification of renal cell cancers in patients with von hippel-lindau disease (vhl). |
1991-06-13 |
2023-08-11 |
Not clear |
| E R Maher, E Bentley, J R Yates, D Barton, A Jennings, I W Fellows, M A Ponder, B A Ponder, C Benjamin, R Harri. Mapping of von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis. Journal of the neurological sciences. vol 100. issue 1-2. 1991-05-28. PMID:1982450. |
genetic linkage studies were performed in 12 british families with von hippel-lindau disease (vhl) using rflps at three loci (dnf15s2, thrb, raf1) on the short arm of chromosome 3. |
1991-05-28 |
2023-08-11 |
Not clear |
| B R Seizinger, D I Smith, M R Filling-Katz, H Neumann, J S Green, P L Choyke, K M Anderson, R N Freiman, S M Klauck, J Whale. Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease. Proceedings of the National Academy of Sciences of the United States of America. vol 88. issue 7. 1991-05-06. PMID:2011596. |
von hippel lindau disease (vhl) is a hereditary syndrome, associated with tumors and cysts in multiple organ systems, whose expression and age of onset are highly variable. |
1991-05-06 |
2023-08-11 |
Not clear |
| S Hosoe, H Brauch, F Latif, G Glenn, L Daniel, S Bale, P Choyke, M Gorin, E Oldfield, A Berma. Localization of the von Hippel-Lindau disease gene to a small region of chromosome 3. Genomics. vol 8. issue 4. 1991-03-05. PMID:2276737. |
we studied 25 families with von hippel-lindau disease (vhl) to locate vhl more precisely on chromosome 3. |
1991-03-05 |
2023-08-11 |
Not clear |
| M R Filling-Katz, P L Choyke, E Oldfield, L Charnas, N J Patronas, G M Glenn, M B Gorin, J K Morgan, W M Linehan, B R Seizinge. Central nervous system involvement in Von Hippel-Lindau disease. Neurology. vol 41. issue 1. 1991-02-07. PMID:1985294. |
fifty individuals with von hippel-lindau disease (vhl) were studied with gadolinium-enhanced magnetic resonance imaging (mri) to determine the frequency and distribution of cns lesions. |
1991-02-07 |
2023-08-11 |
Not clear |
| U S Bergerheim, B Frisk, B Stellan, V P Collins, L Zec. del(3p)(p13p21) in renal cell adenoma and del(4p)(p14) in bilateral renal cell carcinoma in two unrelated patients with von Hippel-Lindau disease. Cancer genetics and cytogenetics. vol 49. issue 1. 1990-10-18. PMID:2397466. |
both patients belonged to families with von hippel-lindau disease (vhl). |
1990-10-18 |
2023-08-11 |
Not clear |
| M R Filling-Katz, P L Choyke, N J Patronas, M B Gorin, D Barba, R Chang, J L Doppman, B Seizinger, E H Oldfiel. Radiologic screening for von Hippel-Lindau disease: the role of Gd-DTPA enhanced MR imaging of the CNS. Journal of computer assisted tomography. vol 13. issue 5. 1989-10-19. PMID:2778131. |
thirty-seven members of a family with von hippel-lindau disease (vhl) were prospectively screen for cns hemangioblastomas; 10 family members were previously known to have vhl. |
1989-10-19 |
2023-08-11 |
Not clear |
| C M Jennings, P A Gaine. The abdominal manifestation of von Hippel-Lindau disease and a radiological screening protocol for an affected family. Clinical radiology. vol 39. issue 4. 1988-11-29. PMID:3052992. |
the mortality in von hippel-lindau disease (vhl) is due to the development of central nervous system or abdominal malignancies, particularly renal cell carcinomas. |
1988-11-29 |
2023-08-11 |
Not clear |
| B R Seizinger, G A Rouleau, L J Ozelius, A H Lane, G E Farmer, J M Lamiell, J Haines, J W Yuen, D Collins, D Majoor-Krakaue. Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma. Nature. vol 332. issue 6161. 1988-04-20. PMID:2894613. |
von hippel-lindau disease (vhl) is an autosomal dominant disorder with inherited susceptibility to various forms of cancer, including hemangioblastomas of the central nervous system, phaeochromocytomas, pancreatic malignancies, and renal cell carcinomas. |
1988-04-20 |
2023-08-11 |
human |
| R C Go, J M Lamiell, Y E Hsia, J W Yuen, Y Pai. Segregation and linkage analyses of von Hippel Lindau disease among 220 descendants from one kindred. American journal of human genetics. vol 36. issue 1. 1984-03-05. PMID:6582782. |
von hippel lindau disease (vhl), an autosomal dominant precancerous condition, had segregated in a large kindred. |
1984-03-05 |
2023-08-12 |
Not clear |